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Results 1 - 10 of 92 for Congenital blindness
  1. Autosomal recessive congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light ...
  2. ... Kraft TW, Gross AK. 1 rhodopsin mutations in congenital night blindness. Adv Exp Med Biol. 2010;664:263-72. ...
  3. X-linked congenital stationary night blindness is a disorder of the retina, which is the specialized tissue at the back of the eye that detects light and ...
  4. ... Amaurosis, Leber congenital Congenital amaurosis of retinal origin Congenital retinal blindness CRB Dysgenesis neuroepithelialis retinae Hereditary epithelial dysplasia of ...
  5. Visual Impairment (Nemours Foundation)  
    ... loss, visual problems, eyes, eyesight, sight, sigt, seeing, congenital blindness, retina, cornea, iris, lens, braille, eye injuries, seeing-eye dog, seeing-eye dogs, guide dog, ...
  6. ... Kraft TW, Gross AK. 1 rhodopsin mutations in congenital night blindness. Adv Exp Med Biol. 2010;664:263-72. ...
  7. ... have been identified in people with X-linked congenital stationary night blindness. Mutations in this gene are responsible for the ... vision problems similar to those of X-linked congenital stationary night blindness.Researchers have identified at least one CACNA1F mutation ...
  8. ... have been identified in people with X-linked congenital stationary night blindness. Mutations in this gene are responsible for the ... the other vision problems characteristic of X-linked congenital stationary night blindness. The mutations responsible for high myopia each change ...
  9. ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... is mutated in patients with autosomal-recessive complete congenital stationary night blindness. Am J Hum Genet. 2009 Nov;85(5): ...
  10. ... gene have been found to cause autosomal recessive congenital stationary night blindness, which is characterized by the inability to see ... coupling in an mGluR6 point mutant associated with congenital stationary night blindness. Mol Pharmacol. 2009 Nov;76(5):992-7. ...
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